Structure differentiation of hydrophilic brass nanoparticles using a polyol toolbox
Structure differentiation of hydrophilic brass nanoparticles using a polyol toolbox
Nano-brasses are emerging as a new class of composition-dependent applicable materials. It remains a challenge to synthesize hydrophilic brass nanoparticles (NPs) and further exploit them for promising bio-applications. Based on red/ox potential of polyol and nitrate salts precursors, a series of hydrophilic brass formulations of different nanoarchitectures was prepared and characterized. Self-assembly synthesis was performed in the presence of triethylene glycol (TrEG) and nitrate precursors Cu(NO3)2·3H2O and Zn(NO3)2·6H2O in an autoclave system, at different temperatures, conventional or microwave-assisted heating, while a range of precursor ratios was investigated. NPs were thoroughly characterized via X-ray diffraction (XRD), thermogravimetric analysis (TGA), scanning electron microscopy (SEM), transmition electron microscopy (TEM), Fourier-transform infrared (FTIR) spectroscopy, dynamic light scattering (DLS), and ζ-potential to determine the crystal structure, composition, morphology, size, state of polyol coating, and aqueous colloidal stability. Distinct bimetallic α-brasses and γ-brasses, α-Cu40Zn25/γ-Cu11Zn24, α-Cu63Zn37, α-Cu47Zn10/γ-Cu19Zn24, and hierarchical core/shell structures, α-Cu59Zn30@(ZnO)11, Cu35Zn16@(ZnO)49, α-Cu37Zn18@(ZnO)45, Cu@Zinc oxalate, were produced by each synthetic protocol as stoichiometric, copper-rich, and/or zinc-rich nanomaterials. TEM sizes were estimated at 20–40 nm for pure bimetallic particles and at 45–70 nm for hierarchical core/shell structures. Crystallite sizes for the bimetallic nanocrystals were found ca. 30–45 nm, while in the case of the core-shell structures, smaller values around 15–20 nm were calculated for the ZnO shells. Oxidation and/or fragmentation of TrEG was unveiled and attributed to the different fabrication routes and formation mechanisms. All NPs were hydrophilic with 20–30% w/w of polyol coating, non-ionic colloidal stabilization (−5 mV < ζ-potential < −13 mV) and relatively small hydrodynamic sizes (<250 nm). The polyol toolbox proved effective in tailoring the structure and composition of hydrophilic brass NPs while keeping the crystallite and hydrodynamic sizes fixed.
Antonoglou, Orestis
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Founta, Evangelia
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Karagkounis, Vasilis
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Pavlidou, Eleni
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Litsardakis, George
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Mourdikoudis, Stefanos
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Thanh, Nguyen Thi Kim
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Dendrinou-Samara, Catherine
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29 November 2019
Antonoglou, Orestis
ab3f7e90-0950-4372-91a5-d5b74496f9d9
Founta, Evangelia
71ba6e64-92a2-4222-9c4e-cf4c7fd8ad97
Karagkounis, Vasilis
65eed5a0-a1c7-4b92-9211-8281c366dcf8
Pavlidou, Eleni
14ab1348-9117-40a7-8ec2-39df2b890b9b
Litsardakis, George
02691802-c73a-4253-857b-fb3fe6200263
Mourdikoudis, Stefanos
c1f812b8-0082-476d-92ed-c61989aaa4ac
Thanh, Nguyen Thi Kim
1d27f7a9-3390-4b16-bfa2-cfb2fa0343c4
Dendrinou-Samara, Catherine
d8b4368c-470a-45e7-86b4-1798eae781b5
Antonoglou, Orestis, Founta, Evangelia, Karagkounis, Vasilis, Pavlidou, Eleni, Litsardakis, George, Mourdikoudis, Stefanos, Thanh, Nguyen Thi Kim and Dendrinou-Samara, Catherine
(2019)
Structure differentiation of hydrophilic brass nanoparticles using a polyol toolbox.
Frontiers in Chemistry, 7 (817).
(doi:10.3389/fchem.2019.00817).
Abstract
Nano-brasses are emerging as a new class of composition-dependent applicable materials. It remains a challenge to synthesize hydrophilic brass nanoparticles (NPs) and further exploit them for promising bio-applications. Based on red/ox potential of polyol and nitrate salts precursors, a series of hydrophilic brass formulations of different nanoarchitectures was prepared and characterized. Self-assembly synthesis was performed in the presence of triethylene glycol (TrEG) and nitrate precursors Cu(NO3)2·3H2O and Zn(NO3)2·6H2O in an autoclave system, at different temperatures, conventional or microwave-assisted heating, while a range of precursor ratios was investigated. NPs were thoroughly characterized via X-ray diffraction (XRD), thermogravimetric analysis (TGA), scanning electron microscopy (SEM), transmition electron microscopy (TEM), Fourier-transform infrared (FTIR) spectroscopy, dynamic light scattering (DLS), and ζ-potential to determine the crystal structure, composition, morphology, size, state of polyol coating, and aqueous colloidal stability. Distinct bimetallic α-brasses and γ-brasses, α-Cu40Zn25/γ-Cu11Zn24, α-Cu63Zn37, α-Cu47Zn10/γ-Cu19Zn24, and hierarchical core/shell structures, α-Cu59Zn30@(ZnO)11, Cu35Zn16@(ZnO)49, α-Cu37Zn18@(ZnO)45, Cu@Zinc oxalate, were produced by each synthetic protocol as stoichiometric, copper-rich, and/or zinc-rich nanomaterials. TEM sizes were estimated at 20–40 nm for pure bimetallic particles and at 45–70 nm for hierarchical core/shell structures. Crystallite sizes for the bimetallic nanocrystals were found ca. 30–45 nm, while in the case of the core-shell structures, smaller values around 15–20 nm were calculated for the ZnO shells. Oxidation and/or fragmentation of TrEG was unveiled and attributed to the different fabrication routes and formation mechanisms. All NPs were hydrophilic with 20–30% w/w of polyol coating, non-ionic colloidal stabilization (−5 mV < ζ-potential < −13 mV) and relatively small hydrodynamic sizes (<250 nm). The polyol toolbox proved effective in tailoring the structure and composition of hydrophilic brass NPs while keeping the crystallite and hydrodynamic sizes fixed.
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fchem-07-00817
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Accepted/In Press date: 12 November 2019
Published date: 29 November 2019
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Local EPrints ID: 501057
URI: http://eprints.soton.ac.uk/id/eprint/501057
ISSN: 2296-2646
PURE UUID: 9f61e2d3-ae9d-4806-bb23-a5188af4992e
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Date deposited: 21 May 2025 16:46
Last modified: 22 May 2025 02:14
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Author:
Orestis Antonoglou
Author:
Evangelia Founta
Author:
Vasilis Karagkounis
Author:
Eleni Pavlidou
Author:
George Litsardakis
Author:
Stefanos Mourdikoudis
Author:
Nguyen Thi Kim Thanh
Author:
Catherine Dendrinou-Samara
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